GE HealthCare Technologies recently expanded its PETtrace Solid Target Platform to support Copper-64 production and secured ...

MINItrace Magni is an automated, self-shielded cyclotron developed for in-house radioisotope manufacturing.

Aptar Announces CE marking for LuerVax® and Accompanying Spray Divider, Strengthening Support for Vaccine Developers ...

The Lumee Oxygen Platform is designed to provide continuous, real-time monitoring of tissue oxygen levels through Profusa's proprietary tissue-integrated biosensor technology. The platform is intended ...

With the ever-increasing stringency, time, and expense associated with FDA approval for medical devices, debate is sharpening in the medical devices industry over whether it is actually better ...

The CE mark suspension isn’t the first setback the Cardiosave intra-aortic balloon pumps have faced in recent months. In December, Getinge began a recall of the pumps that was ultimately given the FDA ...

The CE Mark under the European Union's Medical Device Regulation (MDR 2017/745) standards certifies compliance with stringent health, safety, and environmental protection standards required for ...

The labels on your gadgets can convey critical information about safe usage, so it's a smart practice to understand the meanings of all the different symbols and icons you might see there. One logo ...

TUCSON, Ariz., May 13, 2014 /PRNewswire/ -- On April 17, 2014, SynCardia Systems, Inc. received the CE Mark for the SynCardia temporary Total Artificial Heart with SynHall™ valves, providing the ...